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- Date of registration
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EUDAMED last updated this device on May 24, 2026
69319181F072LA80-05810 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by GRI Medical & Electronic Technology Co., Ltd.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
1693191817442669319181F072LA80-05810(01)16931918174426
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
T020199SURGICAL DRAPES - OTHER1 warning recorded — scroll inside the panel to see all entries.
CW009No certificate specifically references this device's Basic UDI-DI.
Primary placement in Netherlands; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Still on market |
CN-MF-000004203No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.